SIRT1 Functionally Interacts with the Metabolic Regulator and Transcriptional Coactivator PGC-1α

Oxidants, oxidative stress and the biology of ageing

Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413

Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1

Wu, Z., Puigserver, P., Andersson, U., Zhang, C., Adelmant, G., Mootha, V., Troy, A., Cinti, S., Lowell, B., Scarpulla, R. C., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80611-x · Cited by 4,139

Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase

Imai, S.-I., Armstrong, C. M., Kaeberlein, M., & Guarente, L. (2000) · Nature · doi:10.1038/35001622 · Cited by 3,510

Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase

Brunet, A., Sweeney, L. B., Sturgill, J. F., Chua, K. F., Greer, P. L., Lin, Y., Tran, H., Ross, S. E., Mostoslavsky, R., Cohen, H. Y., et al. (2004) · Science · doi:10.1126/science.1094637 · Cited by 3,239

Modulation of NF‐κB‐dependent transcription and cell survival by the SIRT1 deacetylase

Yeung, F., Hoberg, J. E., Ramsey, C. S., Keller, M. D., Jones, D. R., Frye, R. A., & Mayo, M. W. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600244 · Cited by 2,750

hSIR2SIRT1 Functions as an NAD-Dependent p53 Deacetylase

Vaziri, H., Dessain, S. K., Eaton, E. N., Imai, S., Frye, R. A., Pandita, T. K., Guarente, L., & Weinberg, R. A. (2001) · Cell · doi:10.1016/s0092-8674(01)00527-x · Cited by 2,690

The SIR2/3/4 complex and SIR2 alone promote longevity in Saccharomyces cerevisiae by two different mechanisms

Kaeberlein, M., McVey, M., & Guarente, L. (1999) · Genes & Development · doi:10.1101/gad.13.19.2570 · Cited by 2,253

Negative Control of p53 by Sir2α Promotes Cell Survival under Stress

Luo, J., Nikolaev, A. Y., Imai, S.-I., Chen, D., Su, F., Shiloh, A., Guarente, L., & Gu, W. (2001) · Cell · doi:10.1016/s0092-8674(01)00524-4 · Cited by 2,081

Peroxisome Proliferator-Activated Receptor-γ Coactivator 1α (PGC-1α): Transcriptional Coactivator and Metabolic Regulator

Puigserver, P., & Spiegelman, B. M. (2003) · Endocrine Reviews · doi:10.1210/er.2002-0012 · Cited by 2,076

Calorie restriction promotes mammalian cell survival by inducing the SIRT1 deacetylase

Cohen, H. Y., Miller, C., Bitterman, K. J., Wall, N. R., Hekking, B., Kessler, B., Howitz, K. T., Gorospe, M., de Cabo, R., & Sinclair, D. A. (2004) · Science · doi:10.1126/science.1099196 · Cited by 1,924

Nutrient-Dependent Acetylation Controls Basic Regulatory Metabolic Switches and Cellular ReprogrammingPreprint

Dominy, J. E., Gerhart‐Hines, Z., & Puigserver, P. (2011) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2012.76.010843 · Cited by 12

Targeting Epigenetic Regulators with HDAC and BET Inhibitors to Modulate Muscle Wasting

Nevi, L., Pöllänen, N., Penna, F., & Caretti, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242216404 · Cited by 11

Withania somnifera Regulates Mitochondrial Biogenesis and Energetics in Rat Cortical Neurons: Role of BDNF and SIRT1

Fanibunda, S. E., Kukkemane, K., Ghai, U., Kolthur‐Seetharam, U., Hingorani, L., Vaidya, A. D. B., & Vaidya, V. A. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-04920-7 · Cited by 14

Calorie restriction upregulated sirtuin 1 by attenuating its ubiquitin degradation in cancer cells

Han, L., Zhao, G., Wang, H., Tong, T., & Chen, J. (2014) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12199 · Cited by 11

SILAC-Based Quantification of Sirt1-Responsive Lysine Acetylome

Chen, Y., Colak, G., & Zhao, Y. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-637-5_7 · Cited by 11

Nicotinamide and resveratrol regulate bovine adipogenesis through a SIRT1-dependent mechanism

Li, M., Sun, X., Zhou, Y., Wei, X., Sun, Y., Lan, X., Lei, C., & Chen, H. (2015) · Journal of Functional Foods · doi:10.1016/j.jff.2015.08.008 · Cited by 11

Novel modulators of hepatosteatosis, inflammation and fibrogenesis

Lakshman, M., Reyes‐Gordillo, K., Varatharajalu, R., Arellanes‐Robledo, J., Leckey, L. C., Garige, M., & Shah, R. (2014) · Hepatology International · doi:10.1007/s12072-014-9526-8 · Cited by 11

Metabolic Reprogramming via Targeting CD38 NADase Augments Adoptive T Cell Therapy

Fernandez, M. R., & Cleveland, J. L. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.12.014 · Cited by 11

Protective effect of dietary fiber from sweet potato (Ipomoea batatasL.) against lead-induced renal injury by inhibiting oxidative stress via AMPK/SIRT1/PGC1α signaling pathways

Zhang, Y., Gu, W., Duan, L., Zhu, H., Wang, H., Wang, J., Sun, J. G., & Niu, F. (2018) · Journal of Food Biochemistry · doi:10.1111/jfbc.12513 · Cited by 11

ERK Dephosphorylation through MKP1 Deacetylation by SIRT1 Attenuates RAS-Driven Tumorigenesis

Kwon, O., Lee, H., Kim, Y.-J., Cha, H., Song, N., & Lee, M. (2020) · Cancers · doi:10.3390/cancers12040909 · Cited by 11

Muscle‐specific sirtuin1 gain‐of‐function ameliorates skeletal muscle atrophy in a pre‐clinical mouse model of cerebral ischemic stroke

Tuntevski, K., Hajira, A., Nichols, A., Alway, S. E., & Mohamed, J. S. (2020) · FASEB BioAdvances · doi:10.1096/fba.2020-00017 · Cited by 10

Nutraceutical and pharmaceutical cocktails did not preserve diaphragm muscle function or reduce muscle damage in D2‐mdx mice

Spaulding, H. R., Quindry, T. S., Quindry, J. C., & Selsby, J. T. (2020) · Experimental Physiology · doi:10.1113/ep087887 · Cited by 11

Longevity and Aging in Budding Yeast

Kaeberlein, M. R. (2006) · Elsevier eBooks · doi:10.1016/b978-012369391-4/50019-9 · Cited by 12

Disruption of histone acetylation homeostasis triggers cognitive dysfunction in experimental diabetes

Aggarwal, A., Yadav, B., Sharma, N., Kaur, R., & Rishi, V. (2023) · Neurochemistry International · doi:10.1016/j.neuint.2023.105592 · Cited by 10

SIRT1 regulates hepatic vldlr levels

Peyman, M., Gonçalves, A. B.-E., Rodríguez‐Rodríguez, R., Rigon, M., Aguilar-Recarte, D., Villarroya, J., Planavila, A., Villarroya, F., Palomer, X., Barroso, E., et al. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01666-y · Cited by 10

Distinctive effects of licarin A on lipolysis mediated by PKA and on formation of brown adipocytes from C3H10T1/2 mesenchymal stem cells

Yoon, D., Imran, K. M., & Kim, Y. (2017) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2017.12.015 · Cited by 10

Whey protein protects liver mitochondrial function against oxidative stress in rats exposed to acrolein

Aydın, B., Oğuz, A., Şekeroğlu, V., & Şekeroğlu, Z. A. (2022) · Archives of Industrial Hygiene and Toxicology · doi:10.2478/aiht-2022-73-3640 · Cited by 10

Anti-steatotic linagliptin pleiotropic effects encompasses suppression of de novo lipogenesis and ER stress in high-fat-fed mice

Santos, F., Correia, B. R. O., Marinho, T. D. S., Barbosa‐da‐Silva, S., Mandarim‐de‐Lacerda, C. A., & Souza‐Mello, V. (2020) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2020.110804 · Cited by 11

Comparing Acute, High Dietary Protein and Carbohydrate Intake on Transcriptional Biomarkers, Fuel Utilisation and Exercise Performance in Trained Male Runners

Furber, M., Pyle, S., Roberts, M. G., & Roberts, J. (2021) · Nutrients · doi:10.3390/nu13124391 · Cited by 12

Protective effect of ginsenoside Rd on military aviation noise-induced cochlear hair cell damage in guinea pigs

Chen, X., Liu, Y., Ji, S., Xue, X., Wang, L., Zhang, M., Chang, Y., & Wang, X.-C. (2022) · Environmental Science and Pollution Research · doi:10.1007/s11356-022-23504-9 · Cited by 10

Is systemic activation of Sirt1 beneficial for ageing-associated metabolic disorders?

Tang, B. L., & Chua, C. E. L. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.11.016 · Cited by 10

The therapeutic potential of a calorie-restricted ketogenic diet for the management of Leber hereditary optic neuropathy

Storoni, M., Robert, M. P. A., & Plant, G. T. (2017) · Nutritional Neuroscience · doi:10.1080/1028415x.2017.1368170 · Cited by 10

SIRT 1 binding with PKM and NSE and modulate their acetylation and activities

Zhang, Z., Zhang, H., Wang, Y., Liu, X.-L., Huang, H., & Xu, X. (2019) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2019.06.003 · Cited by 10

The impact of a 48-h fast on SIRT1 and GCN5 in human skeletal muscle

Edgett, B. A., Scribbans, T. D., Raleigh, J. P., Matusiak, J. B. L., Boonstra, K. M., Simpson, C. A., Perry, C. G. R., Quadrilatero, J., & Gurd, B. J. (2016) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2016-0130 · Cited by 10

Longevity

Bushell, W. C. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04538.x · Cited by 10

Hypothalamus–Muscle Parallel Induction of Metabolic Pathways Following Physical Exercise

Katz, A., Gonen, M., Shahar, Y., Roichman, A., Lerrer, B., & Cohen, H. Y. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.897005 · Cited by 9

Garcinol Promotes the Formation of Slow-Twitch Muscle Fibers by Inhibiting p300-Dependent Acetylation of PGC-1α

Yao, W., Guo, B., Bao, Z., Huang, L., Wang, T., Wen, S., Jin, T., Yu, X., & Huang, F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032702 · Cited by 9

Cisplatin triggers oxidative stress, apoptosis and pro‐inflammatory responses by inhibiting the SIRT1 ‐mediated Nrf2 pathway in chondrocytes

Hsieh, P., Tsai, K., Chou, W.-C., Wu, C., Jou, I., Tu, Y., & Ma, C. (2023) · Environmental Toxicology · doi:10.1002/tox.23885 · Cited by 9

Mitochondrial redox state, bioenergetics, and calcium transport in caloric restriction: A metabolic nexus

Vilas‐Boas, E. A., & Kowaltowski, A. J. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.04.234 · Cited by 9

O-GlcNAcylation of SIRT1 Protects against Cold Stress-Induced Skeletal Muscle Damage via Amelioration of Mitochondrial Homeostasis

Cao, Y., Zhang, M., Li, Y., Lu, J., Zhou, W., Li, X., Shi, H., Xu, B., & Li, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232314520 · Cited by 10

Melanocortin 4 Receptor Activation Attenuates Mitochondrial Dysfunction in Skeletal Muscle of Diabetic Rats

Zhang, H., Liu, J., Qin, G., Li, X., Du, P., Xiao, H., Zhao, D., Tian, T., Wu, J., Yun, M., et al. (2017) · Journal of Cellular Biochemistry · doi:10.1002/jcb.26062 · Cited by 9

Telomeres and SIRT1 as Biomarkers of Gamete Oxidative Stress, Fertility, and Potential IVF Outcome

Pańczyszyn, A., Boniewska‐Bernacka, E., Wertel, I., Sadakierska−Chudy, A., & Goc, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168652 · Cited by 9

Genetic and Pathophysiological Basis of Cardiac and Skeletal Muscle Laminopathies

Bhide, S., Chandran, S., Rajasekaran, N. S., & Melkani, G. C. (2024) · Genes · doi:10.3390/genes15081095 · Cited by 9

Running exercise alleviates depressive-like behaviors through the activation of PINK1-Parkin mediated mitophagy in mice exposed to chronic social defeat stress

Sun, L., Wu, L., Xu, Z., Zeng, W., & Wang, Y. (2025) · Psychiatry Research · doi:10.1016/j.psychres.2025.116714 · Cited by 9

Multifactorial mechanisms of obesity-related HFpEF: the central role of epicardial adipose tissue and therapeutic perspectives

Zhou, Y., Yan, H., Zhu, Y., Jiang, W., & Zhang, S. (2025) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2025.1701459 · Cited by 8

Nutritional Strategies and Aging: Current Evidence and Future Directions

Castelli, S., Aiello, G., Aiello, V., Massimino, E., Pieri, M., Amoah, I., Lombardo, M., Tripodi, G., & Baldelli, S. (2026) · Molecules · doi:10.3390/molecules31050756 · Cited by 9

Nicotinamide-riboside shifts the differentiation of human primary white adipocytes to beige adipocytes impacting substrate preference and uncoupling respiration through SIRT1 activation and mitochondria-derived reactive species production

Nagy, L., Rauch, B., Szerafin, T., Uray, K., Tóth, A., & Bai, P. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.979330 · Cited by 8

Impaired ubiquitin‐proteasome‐mediated PGC ‐1α protein turnover and induced mitochondrial biogenesis secondary to complex‐ I deficiency

Farhoud, M. H., Nijtmans, L. G. J., Wanders, R. J. A., Wessels, H. J. C. T., Lasonder, E., Janssen, A. J. M., Rodenburg, R. J., van den Heuvel, L. P., & Smeitink, J. A. M. (2012) · PROTEOMICS · doi:10.1002/pmic.201100326 · Cited by 8

Multidrug resistance transporter-1 dysfunction perturbs meiosis and Ca2+ homeostasis in oocytes

Nabi, D., Bosi, D., Gupta, N., Thaker, N. A., Fissore, R. A., & Brayboy, L. M. (2022) · Reproduction · doi:10.1530/rep-22-0192 · Cited by 8

Inhibition of microRNA-200c preserves astrocyte sirtuin-1 and mitofusin-2, and protects against hippocampal neurodegeneration following global cerebral ischemia in mice

Griffiths, B. B., Xu, L., Sun, X., Greer, M., Murray, I., & Stary, C. M. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1014751 · Cited by 8

Short-term dietary restriction ameliorates brain injury after cardiac arrest by modulation of mitochondrial biogenesis and energy metabolism in rats

Zhou, M., Yu, T., Fang, X., Ge, Q., Song, F., Huang, Z., Jiang, L., & Wang, P. (2021) · Annals of Translational Medicine · doi:10.21037/atm-20-3075 · Cited by 8

Oxidants and Ca+2 induce PGC-1α degradation through calpain

Rasbach, K. A., Green, P. T., & Schnellmann, R. G. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.08.003 · Cited by 8

The Roles of Sirt1 in Breast and Gynecologic Malignancies

Ding, J., Ye, M. T., & Zhang, S. (2025) · Biology · doi:10.3390/biology14111510 · Cited by 7

The effect of Sirt1 deficiency on Ca2+ and Na+ regulation in mouse ventricular myocytes

Yang, H., Lin, F., Yang, H., Yu, P., Huang, S., Chen, Y., Tsai, C., & Lin, C. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15327 · Cited by 7

Oral Administration of Nacre Extract from Pearl Oyster Shells Has Anti-Aging Effects on Skin and Muscle, and Extends the Lifespan in SAMP8 Mice

Yamamoto, H., Shimomura, N., & Hasegawa, Y. (2024) · Pharmaceuticals · doi:10.3390/ph17060713 · Cited by 8

The Role of PGC-1α in Digestive System Malignant Tumours

Zhang, Q., Chen, W., Xie, C. L., Dai, X., Ma, J., & Lü, J. (2019) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520619666191105125409 · Cited by 7

MicroRNAomic Transcriptomic Analysis Reveal Deregulation of Clustered Cellular Functions in Human Mesenchymal Stem Cells During in Vitro Passaging

Aung, S.-W., Kasim, N. H. A., Shamsuddin, S. A. A., & Ramasamy, T. S. (2019) · Stem Cell Reviews and Reports · doi:10.1007/s12015-019-09924-0 · Cited by 7

Global Trends in Research of Mitochondrial Biogenesis over past 20 Years: A Bibliometric Analysis

Song, L., Liang, J., Wang, W., Gao, J., Chai, H., Tan, Y. T., Zheng, L., Xue, M., & Shi, D. (2023) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2023/7291284 · Cited by 7

Nature’s Timepiece—Molecular Coordination of Metabolism and Its Impact on Aging

Bednářová, A., Kodrík, D., & Krishnan, N. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14023026 · Cited by 7

Mitochondrial Medicine

Wallace, D. C., Lott, M. T., & Procaccio, V. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-383834-6.00013-6 · Cited by 8

Leptin accelerates BMSC transformation into vertebral epiphyseal plate chondrocytes by activating SENP1 ‐mediated deSUMOylation of SIRT3

Li, X., Fu, X., Li, H., Gao, Y., Wang, W., Liu, Z., & Shen, Y. (2022) · FEBS Open Bio · doi:10.1002/2211-5463.13539 · Cited by 7

Genetic Dissection of the Physiological Role of Skeletal Muscle in Metabolic Syndrome

Hagiwara, N. (2014) · New Journal of Science · doi:10.1155/2014/635146 · Cited by 8

Modulating oxidative stress: a reliable strategy for coping with community-acquired pneumonia in older adults

Mao, W., Liu, X., Fan, S., Zhang, R., Liu, M., & Xiao, S. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1549658 · Cited by 8

Inhibiting miR-200a-3p Increases Sirtuin 1 and Mitigates Kidney Injury in a Tubular Cell Model of Diabetes and Hypertension-Related Renal Damage

Martínez-Arroyo, O., Flores-Chova, A., Mendez-Debaets, M., Garcia-Ferran, L., Escrivá, L., Forner, M. J., Redón, J., Cortés, R., & Ortega, A. (2025) · Biomolecules · doi:10.3390/biom15070995 · Cited by 6

Alterations in Energy Metabolism, Mitochondrial Function and Redox Homeostasis in GK Diabetic Rat Tissues Treated with Aspirin

John, A., Amiri, L., Shafarin, J., Tariq, S., Adeghate, E. A., Howarth, F. C., & Raza, H. (2022) · Life · doi:10.3390/life12010104 · Cited by 6

Sirtuins: Role in the Regulation of Oxidative Stress and the Pathogenesis of Neurodegenerative Diseases

Pukhalskaia, A. E., Diatlova, A., Linkova, N. S., & Kvetnoy, I. M. (2022) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-022-01217-3 · Cited by 6

Comparing the mitochondrial signatures in ESCs and iPSCs and their neural derivations

Kristiansen, C. K., Chen, A., Høyland, L. E., Ziegler, M., Sullivan, G. J., Bindoff, L. A., & Liang, K. X. (2022) · Cell Cycle · doi:10.1080/15384101.2022.2092185 · Cited by 6

Emerging Roles of Signal Transduction Pathways in Neurodegenerative Diseases. Hunting New Possible Therapeutic Molecular Targets

Vasco, V. R. L. (2023) · OBM Geriatrics · doi:10.21926/obm.geriatr.2302234 · Cited by 6

Protection of the rat brain from hypothermic circulatory arrest injury by a chipmunk protein

Jiang, X., Gu, T., Liu, Y., Wang, C., Shi, E., Zhang, G., & Xiu, Z. (2018) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2018.02.048 · Cited by 6

Response of the Sirtuin/PXR signaling pathway in Mugilogobius chulae exposed to environmentally relevant concentration Paracetamol

Xie, M., Wang, Y., Wang, C., Tianli, T., Li, J., Peng, Y., & Xiangping, N. (2022) · Aquatic Toxicology · doi:10.1016/j.aquatox.2022.106222 · Cited by 6

Cellular NAD+Level: A Key Determinant of Mitochondrial Quality and Health

Hwang, E. S., & Hwang, S. Y. (2017) · Annals of Geriatric Medicine and Research · doi:10.4235/agmr.2017.21.4.149 · Cited by 6

Cellular Mechanisms of Endocrine Disruption

Adler, S. (2007) · Humana Press eBooks · doi:10.1007/1-59745-107-x_6 · Cited by 11

The role of nicotinamide riboside in the preservation of retinal ganglion cells using an in vitro glutamate-induced excitotoxicity model

Zhang, N., Ji, D., Hu, Y., Zhang, P., Deng, X., Zhu, M., Zeng, W., & Ke, M. (2024) · Experimental Eye Research · doi:10.1016/j.exer.2024.110126 · Cited by 7

Caloric Restriction and Sirtuins as New Players to Reshape Male Fertility

André, D. C. A., Oliveira, P. F., Alves, M. G., & Martins, A. D. (2025) · Metabolites · doi:10.3390/metabo15050303 · Cited by 7

Aerobic exercise attenuates intramyocellular lipid accumulation by upregulating vitamin D receptor

Wang, K., Zhang, J., Cui, X., Niu, Y.-J., Liu, J., Lu, S., Liu, X.-M., Zhu, Z., & Cao, Z. (2025) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2025.112677 · Cited by 5

Mitochondrial Adaptation to Mechanical Stress in Cardiac Ageing and Disease

Prakash, A., & Iskratsch, T. (2025) · Advanced Science · doi:10.1002/advs.202516736 · Cited by 5

Components of Panax ginseng and Rhodiola rosea regulate mitophagy via the SIRT1/3-PGC-1α-NRF2 pathway to improve myocardial ischemia-reperfusion injury

Yao, M., Wang, X., Wei, H., Wang, L., Zhang, D., Liang, Z., He, R., He, Y., Jiang, L., & Cui, Y. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1716078 · Cited by 5

Molecular Dialogues in the Mitochondria–Microbiome Crosstalk: Metabolites, Signaling, and Immunity

Tenchov, R. (2026) · Comprehensive physiology · doi:10.1002/cph4.70164 · Cited by 6

SIRT1 and SIRT3 Impact Host Mitochondrial Function and Host Salmonella pH Balance during Infection

Hajra, D., Yadav, V., Singh, A., & Chakravortty, D. (2025) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.4c00751 · Cited by 5

Brain Region and Sex-specific Changes in Mitochondrial Biogenesis Induced by Acute Trimethyltin Exposure

Lee, J. H., Jang, E. H., & Kim, S. A. (2022) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2022.20.3.474 · Cited by 6

PPARgamma dependent PEX11beta counteracts the suppressive role of SIRT1 on neural differentiation of HESCs

Esmaeili, M., Nasr‐Esfahani, M. H., Nejati, A. S., Safaeinejad, Z., Atefi, A., Megraw, T. L., & Ghaedi, K. (2024) · PLoS ONE · doi:10.1371/journal.pone.0298274 · Cited by 5

Sirtuin and Resveratrol

Pallàs, M., Sanfeliu, C., Pelegrı́, C., Cristòfol, R. M., Camins, A., Mercè, & Vilaplana, J. (2009) · Oxidative stress and disease · doi:10.1201/9781420073522.ch22 · Cited by 5

Down-regulation of bile acid synthesis and a metabolic co-activator under hypoxic conditions – implications in obstructive sleep apnea

Johnson, P. R. (2008) · Medical Hypotheses · doi:10.1016/j.mehy.2008.02.021 · Cited by 5

Small Molecule Modulators of Sirtuin Activity

Alcain, F. J., Minor, R. K., Villalba, J. M., & de Cabo, R. (2010) · Springer eBooks · doi:10.1007/978-90-481-3999-6_10 · Cited by 5

The Regulation of the Concentrations of Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-Alpha and Sirtuin 1 Protein in the Soleus Muscle by Aerobic Exercise Training in Obese Wistar Rats

Hejazi, K., Hosseini, S. R. A., Fathi, M., & Ziaaldini, M. M. (2020) · Journal of Kermanshah University of Medical Sciences · doi:10.5812/jkums.101849 · Cited by 5

A MiR181/Sirtuin1 regulatory circuit modulates drug response in biliary cancers

Barbato, A., Piscopo, F., Salati, M., Pollastro, C., Evangelista, L., Ferrante, L., Limongello, D., Brillante, S., Iuliano, A., Bonetti, L. R., et al. (2024) · Clinical and Experimental Medicine · doi:10.1007/s10238-024-01332-0 · Cited by 5

Calorie Restriction and Cancer Prevention: Established and Emerging Mechanisms

Hursting, S. D., Ford, N. A., Dunlap, S. M., Hursting, M. J., & Lashinger, L. M. (2013) · Springer eBooks · doi:10.1007/978-1-4614-6819-6_14 · Cited by 5

Histone Deacetylases ( HDACs ): Function, Mechanism, & Inhibition

Sarkar, S., Longacre, M. M., Tatur, N., Heerboth, S. A., & LAPINSKA, K. (2000) · Wiley eBooks · doi:10.1002/9780470027318.a9365 · Cited by 5

Need for NAD+: Focus on Striated Muscle Laminopathies

Cardoso, D., & Muchir, A. (2020) · Cells · doi:10.3390/cells9102248 · Cited by 5

Biomarkers of Mitochondrial Dysfunction and Toxicity

Palmeira, C. M., Teodoro, J. S., Silva, R., & Rolo, A. P. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814655-2.00055-4 · Cited by 4

Emerging Gene Therapy Technologies for Retinal Ganglion Cell Neuroprotection

Camacho, D. K., Go, C. C., Chaqour, B., Shindler, K. S., & Ross, A. G. (2023) · Journal of Neuro-Ophthalmology · doi:10.1097/wno.0000000000001955 · Cited by 4

Dark tea extract attenuates age-related muscle loss by suppressing oxidative stress and inflammation in skeletal muscle of mice

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